A trans diacyloxylation of indoles
文献类型:期刊论文
| 作者 | Liu Q(刘强)1; Zhao QY(赵庆勇)1; Liu J(刘劼)1; Wu P(巫攀)1; Yi H(易宏)1; Lei AW(雷爱文)1,2 |
| 刊名 | Chemical Communications
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| 出版日期 | 2012 |
| 卷号 | 48期号:26页码:3239-3241 |
| ISSN号 | 1359-7345 |
| 通讯作者 | 雷爱文 |
| 英文摘要 | A trans diacyloxylation of indoles is accomplished by employing PhI(OAc)2 as the oxidant. A broad range of functional groups are well tolerated. Both the electronic properties of the N-protecting groups of indoles and the acidity of the reaction media play important roles in the selectivity of indole acyloxylation reactions. |
| 学科主题 | 物理化学与绿色催化 |
| 收录类别 | SCI |
| 资助信息 | Program for Changjiang Scholars and Innovative Research Team in University (IRT1030);National Natural Science Foundation of China (20972118;20832003);financial support from Wuhan University |
| 语种 | 英语 |
| WOS记录号 | WOS:000300874700029 |
| 公开日期 | 2013-10-11 |
| 源URL | [http://210.77.64.217/handle/362003/3805] ![]() |
| 专题 | 兰州化学物理研究所_OSSO国家重点实验室 |
| 作者单位 | 1.Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China 2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China |
| 推荐引用方式 GB/T 7714 | Liu Q,Zhao QY,Liu J,et al. A trans diacyloxylation of indoles[J]. Chemical Communications,2012,48(26):3239-3241. |
| APA | Liu Q,Zhao QY,Liu J,Wu P,Yi H,&Lei AW.(2012).A trans diacyloxylation of indoles.Chemical Communications,48(26),3239-3241. |
| MLA | Liu Q,et al."A trans diacyloxylation of indoles".Chemical Communications 48.26(2012):3239-3241. |
入库方式: OAI收割
来源:兰州化学物理研究所
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